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NCT Number: NCT07492537

SUBDIMA: Subclinical Depression in Acute Myocardial Infarction (SUBDIMA25)

This is an exploratory, prospective, non-profit study (SUBDIMA) designed to investigate the prevalence and potential prognostic significance of subclinical depression in patients admitted with a first acute myocardial infarction (AMI). Subclinical depression refers to the presence of mild depressive symptoms (PHQ-9 score 5-9) that do not meet DSM-5 TR criteria for major depressive disorder but may still be clinically relevant. The primary aim is to estimate the prevalence of subclinical depression in this setting. Secondary, exploratory objectives include evaluating associations with inflammatory and metabolic biomarkers, autonomic dysfunction, cardiac function, cognitive performance, quality of life, treatment adherence, and the risk of recurrent cardiovascular events over 12 months. The study is expected to generate new descriptive data that may inform future confirmatory trials and support early, personalized approaches to integrated cardiac and mental health care.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Cardiologia

Roma, Italia, 00168, Italy

Location status: Recruiting

Location contact

Fabio Infusino

CONTACT

+390630155701

Fabio Infusino

PRINCIPAL_INVESTIGATOR

About this study

Depression is a recognized risk factor for adverse outcomes in patients with acute coronary syndromes. While most studies have focused on major depressive disorder, subclinical depression (defined as PHQ-9 scores between 5 and 9 in the absence of DSM-5 TR criteria for major depression) remains poorly characterized. Its prevalence in patients with a first acute myocardial infarction (AMI) is largely unknown, as are its potential associations with clinical, biological, and psychosocial outcomes.

The SUBDIMA study is a prospective, exploratory, single-center, non-profit clinical investigation conducted at Fondazione Policlinico Universitario A. Gemelli IRCCS. Consecutively admitted patients with a first AMI will undergo systematic screening with the PHQ-9 and a structured clinical assessment to exclude major depression. Based on these evaluations, patients will be classified into two groups: with or without subclinical depression. All participants will be followed for 12 months, with visits at baseline, 3 months, and 12 months, and intermediate phone contacts at 6 and 9 months.

The primary aim of the study is descriptive: to estimate the prevalence of subclinical depression in this population. Secondary, exploratory aims are to examine potential associations between subclinical depression and:

  • inflammatory and metabolic biomarkers,
  • measures of autonomic dysfunction (e.g., heart rate variability),
  • cardiac function parameters (e.g., echocardiographic strain indices, NT-proBNP),
  • cognitive and anxiety assessments,
  • health-related quality of life and lifestyle factors,
  • adherence to treatment,
  • and the incidence of recurrent cardiovascular events during follow-up.

Given its exploratory design, the study is not powered to test confirmatory hypotheses. Instead, it is expected to provide novel descriptive data that will inform the design of future confirmatory trials and contribute to the integration of psychosocial screening in cardiology care pathways.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥18 years
  • Hospital admission for first acute myocardial infarction (STEMI or NSTEMI) within 7 days from the index event
  • PHQ-9 administered at screening
  • Mini Mental State Examination (MMSE) score ≥26
  • Written informed consent obtained

Exclusion criteria

  • Previous history of acute myocardial infarction
  • Diagnosis of major depression according to DSM-5 TR criteria
  • Severe cognitive impairment (MMSE <26)
  • Severe comorbidities with expected survival <12 months
  • Inability to participate in scheduled follow-up assessments
  • Refusal or inability to provide informed consent
  • Concurrent participation in other interventional clinical studies that could interfere with study outcomes

Treatment and study plan

Psychological, Cognitive, and Patient-Reported Outcome Assessments

Other

Structured evaluation including PHQ-9, BDI-II, HAM-A, cognitive tests (CVLT-2, Matrici Attentive, Rey-Osterrieth), and validated questionnaires (EQ-5D-5L, PSQI, IPAQ, Medi-Lite, MARS-5) administered at baseline and during follow-up (3, 6, 9, and 12 months).

Primary outcomes

  1. Prevalence of Subclinical Depression in Patients with First Acute Myocardial Infarction

    Time frame: Baseline (hospital admission)

    Proportion of patients with PHQ-9 score between 5 and 9 who do not meet DSM-5 TR criteria for major depression among those admitted with first acute myocardial infarction.

Secondary outcomes

  1. C-reactive protein (CRP) levels

    Time frame: Baseline, 3 months, and 12 months

    Differences in C-reactive protein (CRP) levels between patients with and without subclinical depression.

  2. Lipid profile

    Time frame: Baseline, 3 months, and 12 months

    Differences in lipid profile parameters, including total cholesterol, LDL cholesterol, HDL cholesterol, and triglycerides, between patients with and without subclinical depression. Each parameter will be analyzed separately.

  3. NT-proBNP levels

    Time frame: Baseline, 3 months, and 12 months

    Differences in NT-proBNP levels between patients with and without subclinical depression.

  4. Cardiac function (LVEF and GLS)

    Time frame: Baseline, 3 months, and 12 months

    Cardiac function assessed by left ventricular ejection fraction (LVEF) and global longitudinal strain (GLS). Each parameter will be analyzed separately.

  5. Recurrent Cardiovascular Events

    Time frame: Up to 12 months

    Incidence of recurrent ischemic events (AMI, stroke, peripheral ischemia), hospitalization for cardiovascular causes, and cardiovascular mortality.

  6. Quality of Life assessed with EQ-5D-5L and VAS

    Time frame: Baseline, 3 months, and 12 months

    Quality of life assessed using the EuroQol-5D-5L (EQ-5D-5L), including utility index and visual analogue scale (VAS).

  7. Treatment Adherence

    Time frame: Baseline, 3 months, 6 months, 9 months, and 12 months

    Differences in treatment adherence evaluated using the Medication Adherence Report Scale (MARS-5) total score.

  8. Complete blood count (CBC) parameters

    Time frame: Baseline, 3 months, and 12 months

    Differences in complete blood count parameters, including hemoglobin, white blood cell count, and platelet count, between patients with and without subclinical depression. Each parameter will be analyzed separately.

Other outcomes

  1. Sleep Quality assessed with PSQI

    Time frame: Baseline, 3 months, 6 months, 9 months, and 12 months

    Exploratory, descriptive analysis of sleep quality using the Pittsburgh Sleep Quality Index (PSQI).

  2. Physical Activity assessed with IPAQ

    Time frame: Baseline, 3 months, 6 months, 9 months, and 12 months

    Physical activity assessed with International Physical Activity Questionnaire (IPAQ) score.

  3. Dietary Pattern (Medi-Lite Score)

    Time frame: Baseline, 3 months, and 12 months

    Dietary habits assessed with the Medi-Lite Score.

  4. Cognitive function (composite neuropsychological assessment)

    Time frame: Baseline, 3 months, and 12 months

    Cognitive performance assessed using California Verbal Learning Test-II (CVLT-II), Attentive Matrices, and Rey-Osterrieth Complex Figure test.

Study contacts

Contact information is provided by the study sponsor or research team.

Fabio Infusino, MD, PhD

CONTACT

[email protected]

+390630154187

Federica Mammarella, MD, PhD

CONTACT

[email protected]

+390630154187

Sponsors and collaborators

Lead sponsor

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Other

Registry information

Official study title

SUBDIMA Study: Subclinical Depression in Myocardial Infarction -Prevalence, Predictors and Prognostic Impact.

Acronym: SUBDIMA25

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Mar 25, 2026
Registry last updated
Mar 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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